| Tag | Content |
|---|
EnhancerAtlas ID | HS091-33390 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr22:46709910-46711000 |
Target genes | |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CTCF | MA0139.1 | chr22:46710348-46710367 | AGCTGCCATCTAGTGGTAA | - | 6.41 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr22 | 46710661 | 46710723 | | chr22 | 46709981 | 46710583 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH22I046314 | chr22 | 46710281 | 46710430 |
|
Enhancer Sequence | GTGAGGCAGC CGGCATCATG CTTGGACCCA CATCTGGCCA GGTGAGGCCT GGAGTGCTGC 60
TCAGGCCTTG GAGACTGTTT CTGCAGAACC ACTTAGGCTT GGCAGGACGT CCCGGAGGGC 120
GTGCTGTGTG CGGTGGACCA GGCTGTGGAC TGAGTTGCTG TACCTGCCCT CAGTGCCTCT 180
GTCCCATGAG GAGGGCACAC TCAGATGGGT GGCTTCAGTC TACGGGGTAC ACATGGCCAG 240
AAAGCATGTA TGATACCCCG TGCCTGAGAA CATGGACACT GGAATCACCC TCATGTCCAT 300
GTCATGAGAC ACCAGTTTTA AAATAGGACT ATTCCAGATA ATGTAGGGCA TATGGCCCCA 360
TAACTCCTGG GTGCCTGTTT AAATCCATGC TCCCACACCT GTTTGAGGTC AAGCCACATT 420
TCAACCTTGC CAAGCCACAG CTGCCATCTA GTGGTAAGGG AAAGCCTTCG CCTTTCTGCT 480
CTTCAGAGCG AAATCCTCTT CGAGGTGCAT TGGCCATGTG GCGTCTCGGG GTCGTTCAGG 540
GCAGCATGGT GTGGATTGTG TTCACAAAAT GTAAAAAGTG GGCCGGGCGC AGGGGCTCAC 600
GCCTGTGATC CCAGCACTTT GGCAGGCCAA GATGGGTGGA TCGCTTGACC CCTGGAGTTT 660
GAGACCAGCC TGGCCAACAT GGTGAAACCC TGTCTCTACT AAAAACACAA AAACTAGCCG 720
GGCATGGTGG CGGGTGCCTG TAGTCCCAGC TACTCGGGAG ACTGGGCCAC GAGAATGGCT 780
TGAACGCGGG AGGCAGAGGT TACCATGAGC CGAGATTGCA TCACTGCACT CCGTCTCAAA 840
AAAAAAAAAA AAAATGATAA GTGTGAACTC TCTAATCAGA TTGATCTGAT CTGGAATTCT 900
GACTCTGCCA TTCTGTGATT AAGAGAGGTT TGTGTCCTTA TCTTTATAGA CTGAGGTGAT 960
GACCTCCTGA GATCAAGCAA TCCTCCCACC TCAGCCTCCT GAGTAGCTGG GACTACAGGC 1020
ACATGCCACC ACACCCGGCT AATTTTTGTG GGTTTTTTTT TTTTGAGATG GAGTCTCACT 1080
CTATTGCCAG 1090
|
